Clinical and immunohistochemical studies were conducted to evaluate pr
ostatic papillary adenocarcinoma and prostatic papillary hyperplasia.
Subjects consisted of 5 cases of papillary adenocarcinoma and 2 cases
of papillary hyperplasia. There is no conclusive clinical factor for p
reoperative diagnosis, but we attach importance to endoscopic findings
. PSA, PAP, high molecular weight cytokeratin, and PCNA were evaluated
immunohistochemically. PSA became positive in every instance but one-
a case of papillary adenocarcinoma which became +/-.PAP was + in all c
ases, except for 1 case of papillary adenocarcinoma. Basal cells were
positive for high molecular weight cytokeratin in 2 cases of papillary
hyperplasia but were missing in papillary adenocarcinoma. Although PC
NA was free from positive nuclei in papillary hyperplasia, positive nu
clei were found in all cases of papillary adenocarcinoma. Considering
these immunohistochemical results, papillary adenocarcinoma can be sai
d to originate in the glandular epithelium of the prostate, as does or
dinary prostatic carcinoma. (C) 1995 Wiley-Liss, Inc.